Afife UĞUZ, Sema BİRCAN, Şirin BAŞPINAR, Osman ERGUN, Murat DEMİR

BÖBREĞİN JUKSTAGLOMERÜLER HÜCRELİ TÜMÖRÜ: BİR OLGU SUNUMU

Jukstaglomerüler hücreli tümör (JGHT) sekonder hiperaldosteronizme bağlı hipertansiyon ve hipokalemiye neden olan benign renin salgılayan bir tümördür.Genellikle adölesan ve genç erişkinleri etkiler. Klinik olarak tümörlerin çoğu benign bir seyir göstermekle birlikte vasküler invazyon veya metastaz yapan nadir tümörler bildirilmektedir. Burada tekrarlayan baş ağrıları ve hipertansiyonu olan 19 yaşındaki bir kadın hastada JGHT olgusunu sunuyoruz.

JUXTAGLOMERULAR CELL TUMOR OF THE KIDNEY: A CASE REPORT

Juxtaglomerular cell tumor (JGCT) is a benign renin-secreting tumor causing hypertension and hypokalemia due to secondary hyperaldosteronism. It generally affects adolescents and young adults. Clinically, the majority of tumors showed a benign course, but rare tumors with vascular invasion or metastasis were reported. Here we report the case of a JGCT in a 19-year-old female who was suffering from recurrent headaches and hypertension.

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